Clinical Research Associate II
6 dagen geleden
Parexel is in the business of improving the world's health.
We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments. From clinical trials to regulatory, consulting, and market access, our therapeutic, technical, and functional ability is underpinned by a deep conviction in what we do.
We believe in our values, Patients First, Quality, Respect, Empowerment & Accountability.
We are currently recruiting for a Clinical Research Associate II role in our Clinical Operations Team.
This role can be office-based or decentralized in the Netherlands.
Your time here
As a Clinical Research Associate II, you will be accountable for using your expertise to build and maintain the site relationship and ensure they're set up for success. You'll also manage site quality and delivery from site identification through to close-out.
What you'll do
- Conduct qualification visits, site initiation visits, monitoring visits, and termination visits at assigned clinical sites and generate visit/contact reports.
- Build relationships with the site and staff, utilizing problem-solving skills to promote rapport.
- Review the performance of the trial at designated sites, ensuring the rights and well-being of human subjects are safeguarded and in accordance with protocol.
- Develop patient recruitment strategies in conjunction with the clinical site to meet enrollment timelines, while ensuring compliance with the approved standard operating procedures, protocol/amendment(s), GCP, and the applicable regulatory requirement(s).
- Evaluate the quality and integrity of the reported data, site efficacy, and drug accountability.
- Monitor the completeness and quality of Regulatory Documentation and perform site document verification.
More about you
We're looking for someone with site management or equivalent experience in clinical research, with an understanding of clinical trials methodology and terminology. You should be able to perform all clinical monitoring activities independently and have a strong understanding of the Dutch and English languages.
If you're ready to join Parexel's journey, please apply
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